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The Prevalence of COPD in Patients With Cardiovascular Disease and the Benefit of Cardiopulmonary Co-management -A Multi-center, Prospective, Interventional Study (PRECEDE)

Status: Recruiting
Location: See all (85) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a multi-center, prospective, and interventional study conducted in 3 types of cardiovascular diseases (CVD) participants , including 3 cohorts which are patients with newly or previously diagnosed coronary heart disease ( CHD), atrial fibrillation ( AF) and chronic heart failure (CHF).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:

• Give signed written informed consent to participate.

• At least 40 years of age at baseline visit.

• Previous or newly diagnosed by at least one of the 3 types of CVD which are,

‣ Coronary heart disease ( CHD )

⁃ Atrial fibrillation (AF )

⁃ Chronic heart failure ( CHF )

• Participants can undergo spirometry testing and does not have the following serious diseases or disease states:

‣ Shock within the last 3 months

⁃ Mycardial infarction, stroke or unstable angina within last 1 month

⁃ Currently suffering from severe HF or severe arrhythmia. Severe HF refers to the need for intravenous administration of vasoactive drugs and diuretics; severe arrhythmia refers to arrhythmias that cause hemodynamic instability, such as ventricular fibrillation and ventricular tachycardia

⁃ Severe hemoptysis or active gastrointestinal bleeding within last 1 month

⁃ Patients with seizures requiring medication

⁃ Patients with hypertensive crisis or uncontrolled hypertension \[systolic blood pressure \> 200 mmHg, diastolic blood pressure \> 100 mmHg (1 mmHg = 0.133 kPa)\]

⁃ Patients with active respiratory infectious diseases or infectious diseases, such as open pulmonary tuberculosis, influenza, new coronavirus infection, and acute pneumonia

⁃ Patients with aortic or cerebral aneurysms

⁃ Pneumothorax and pneumothorax healing within last 1 month

⁃ Patients with severe hyperthyroidism

⁃ Patients who have recently had eye, ear, cranial or thoracic or abdominal surgery Note: If the patient can cooperate by completing a single, effective forced exhalation (≥6 seconds), then spirometry testing can be performed.

• Subjects have the cognitive ability to conduct questionnaires after e valuated by investigators.

Locations
Other Locations
China
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Anqing
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Beijing
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Beijing
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Beijing
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Beijing
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Beijing
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Changsha
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Changsha
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Chaohu
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Chengdu
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Chengdu
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Chengdu
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Chifeng
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Chongqing
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Dalian
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Dingzhou
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Dongguan
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Foshan
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Fuyang
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Fuzhou
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Ganzhou
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Guanghan
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Guangzhou
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Guangzhou
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Guangzhou
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Guangzhou
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Haikou
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Hangzhou
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Hangzhou
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Harbin
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Harbin
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Hefei
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Hefei
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Hubei
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Jinhua
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Jinzhong
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Jiujiang
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Kaiyuan
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Kunming
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Kunming
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Lanzhou
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Leping
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Lianjiang
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Linhai
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Meizhou
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Mianyang
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Nanchang
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Neijiang
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Ningbo
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Ningbo
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Putian
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Quanzhou
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Shanghai
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Shanghai
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Shanghai
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Shanghai
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Shanghai
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Shantou
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Shantou
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Shenyang
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Shenzhen
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Shijiazhuang
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Sichuan
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Suining
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Suzhou
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Tai’an
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Taiyuan
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Taiyuan
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Tianjin
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Tianjin
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Tianjin
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Tianmen
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Wuhan
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Wuhan
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Wuxi
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Xi'an
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Xiamen
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Xiangyang
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Xinzheng
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Xuzhou
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Yangzhou
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Yulin
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Zhangzhou
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Zhengzhou
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Zunyi
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2025-11-28
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 3000
Treatments
Other: Guideline education and implementation
Sponsors
Leads: AstraZeneca

This content was sourced from clinicaltrials.gov